Cytotoxic rotenoid glycosides from the seeds of Amorpha fruticosa

被引:16
作者
Wu, Xin [1 ]
Liao, Hong-Bo [2 ]
Li, Guo-Qiang [3 ]
Liu, Yi [1 ]
Cui, Liao [1 ]
Wu, Ke-Feng [1 ]
Zhu, Xiao-Hui [4 ]
Zeng, Xiao-Bin [1 ]
机构
[1] Guangdong Med Coll, Guangdong Key Lab Res & Dev Nat Drugs, Zhanjiang 524023, Guangdong, Peoples R China
[2] Guangdong Med Coll, Dept Pharmacol, Zhanjiang 524023, Guangdong, Peoples R China
[3] Jinan Univ, Coll Pharm, Inst Tradit Chinese Med & Nat Prod, Guangzhou 510632, Guangdong, Peoples R China
[4] Guangdong Med Coll, Dept Pathol & Pathophysiol, Zhanjiang 524023, Guangdong, Peoples R China
关键词
Amorpha fruticosa; Rotenoid glycosides; Absolute configuration; Cytotoxic activity; CONSTITUENTS; DERIVATIVES; AGENTS; CELLS; INHIBITOR; GROWTH; FRUITS; ROOTS;
D O I
10.1016/j.fitote.2014.11.015
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Four new rotenoid glycosides, namely amorphaside A-D (1-4), along with four known ones (5-8) were isolated from the seeds of Amorpha fruticosa. Their chemical structures and absolute configurations were elucidated by HRESIMS, NMR and CD spectra, as well as deduction from biosynthesis route. The sugar units were determined by acid hydrolysis, appropriate derivatization and HPLC analysis. The in vitro anti-proliferative activities of all compounds were evaluated against MCF-7 and HCT-116 cell lines. The results showed that compounds 1-3 had no effect on cell proliferation in the two cell lines even with the concentration of 50 mu M, and compounds 4,7 and 8 had selective cytotoxicity against MCF-7 with IC50 values of 3.90, 0.95 and 34.08 mu M, respectively, while compounds Sand 6 both showed significant cytotoxicity to the two cell lines with IC50 values less than 2.00 mu M, even better than the positive control cisplatin. These preliminary results indicated that compounds 5 and 6 might be valuable to anticancer drug candidates. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 80
页数:6
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